FDA Inspection 1249066 — Randox Laboratories Limited

Randox Laboratories Limited — FEI 3014607865

The FDA completed an inspection of Randox Laboratories Limited on Aug 8, 2024 in Antrim. The inspection was classified OAI (Official Action Indicated — regulatory and/or administrative actions are recommended). Product area: Devices.

Inspection Details

Classification
Official Action Indicated (OAI)
End Date
Aug 8, 2024
Fiscal Year
2024
Product Type
Devices
Project Area
Compliance: Devices
Location
Antrim (United Kingdom)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.